Platinum Dissolution in Proton Exchange Membrane Fuel Cell Under Mechanical Vibrations

Author(s):  
Georgiy Diloyan ◽  
Parsaoran Hutapea

One of the factors that affect the performance of proton exchange membrane fuel cells (PEMFC) is the loss of electrochemically active surface area of the Platinum (Pt) based electrocatalyst due to platinum dissolution and sintering. The intent of the current research is to understand the effect of mechanical vibrations on the Pt particles dissolution and overall PEMFC performance. This study is of great importance for the automotive application of fuel cells, since they operate under a vibrating environment. Carbon supported platinum plays an important role as an electrocatalyst in PEMFC. Pt particles, typically a few nanometers in size, are distributed on both cathode and anode sides. Pt particle dissolution and sintering is accelerated by a number of factors, one of which is potential cycling during fuel cell operation. To study the effect of mechanical vibrations on Pt dissolution and sintering, an electrocatalyst (from cathode side) was analyzed by SEM/EDS (Energy Dispersive Spectroscopy). The performance, dissolution and sintering of the Pt particles of 25 cm2 electrocatalyst coated membrane were studied during a series of tests. The experiment was conducted by running three accelerated tests. Each test duration was 300 hours, with different parameters of oscillations: one test without vibrations and remaining two tests under vibrations with frequencies of 20 Hz and 50 Hz (5g of magnitude) respectively. For each of the three tests a pristine membrane was used. The catalyst of each membrane was analyzed by ESEM/EDS in pristine state and in degraded state (after 300 hours of accelerated test). In order to specify the same area of observation on a catalyst before and after accelerated test, a relocation technique was used.

Author(s):  
Isaac Perez-Raya ◽  
Michael W. Ellis ◽  
Abel Hernandez-Guerrero ◽  
Francisco Elizalde-Blancas ◽  
Carlos U. Gonzalez-Valle ◽  
...  

Although fuel cells represent an attractive alternative for electricity generation, different technical problems, such as the hydrogen storage, have not been solved, as yet. Nowadays direct sodium borohydride fuel cells are considered as a promising technology since NaBH4 (fuel) is a stable, nonflammable and nontoxic liquid solution. In the present study a one-dimensional numerical study of a proton exchange membrane, a solid oxide, and a direct sodium borohydride fuel cell is performed. The objective of this work is to compare qualitatively the fuel cell performance between these technologies. For proton exchange membrane and solid oxide fuel cells there are already established useful models and correlations widely known, and used, to predict the current density and the power generated. Direct Borohydride fuel cells, on the other hand, are still in their early developments; in the present paper DBFCs are analyzed using a novel model. This proposed model for DBFCs includes the prediction of the NaBH4 oxidation in the anode side, the H2O2 reduction in the cathode side and the effect of the solution concentration and temperature on the membrane. It is noteworthy mentioning that this last effect has not been integrated in any of the established models in the current technical literature.


2019 ◽  
Author(s):  
Valentina Guccini ◽  
Annika Carlson ◽  
Shun Yu ◽  
Göran Lindbergh ◽  
Rakel Wreland Lindström ◽  
...  

The performance of thin carboxylated cellulose nanofiber-based (CNF) membranes as proton exchange membranes in fuel cells has been measured in-situ as a function of CNF surface charge density (600 and 1550 µmol g<sup>-1</sup>), counterion (H<sup>+</sup>or Na<sup>+</sup>), membrane thickness and fuel cell relative humidity (RH 55 to 95 %). The structural evolution of the membranes as a function of RH as measured by Small Angle X-ray scattering shows that water channels are formed only above 75 % RH. The amount of absorbed water was shown to depend on the membrane surface charge and counter ions (Na<sup>+</sup>or H<sup>+</sup>). The high affinity of CNF for water and the high aspect ratio of the nanofibers, together with a well-defined and homogenous membrane structure, ensures a proton conductivity exceeding 1 mS cm<sup>-1</sup>at 30 °C between 65 and 95 % RH. This is two orders of magnitude larger than previously reported values for cellulose materials and only one order of magnitude lower than Nafion 212. Moreover, the CNF membranes are characterized by a lower hydrogen crossover than Nafion, despite being ≈ 30 % thinner. Thanks to their environmental compatibility and promising fuel cell performance the CNF membranes should be considered for new generation proton exchange membrane fuel cells.<br>


2017 ◽  
Vol 10 (1) ◽  
pp. 96-105 ◽  
Author(s):  
Mohammed Jourdani ◽  
Hamid Mounir ◽  
Abdellatif El Marjani

Background: During last few years, the proton exchange membrane fuel cells (PEMFCs) underwent a huge development. Method: The different contributions to the design, the material of all components and the efficiencies are analyzed. Result: Many technical advances are introduced to increase the PEMFC fuel cell efficiency and lifetime for transportation, stationary and portable utilization. Conclusion: By the last years, the total cost of this system is decreasing. However, the remaining challenges that need to be overcome mean that it will be several years before full commercialization can take place.This paper gives an overview of the recent advancements in the development of Proton Exchange Membrane Fuel cells and remaining challenges of PEMFC.


Author(s):  
Frano Barbir ◽  
Haluk Gorgun ◽  
Xinting Wang

Pressure drop on the cathode side of a PEM (Proton Exchange Membrane) fuel cell stack has been studied and used as a diagnostic tool. Since the Reynolds number at the beginning of the flow field channel was <250, the flow through the channel is laminar, and the relationship between the pressure drop and the flow rate is linear. Some departure from linearity was observed when water was either introduced in the stack or produced inside the stack in the electrochemical reaction. By monitoring the pressure drop in conjunction with the cell resistance in an operational fuel cell stack, it was possible to diagnose either flooding or drying conditions inside the stack.


2015 ◽  
Vol 3 (16) ◽  
pp. 8847-8854 ◽  
Author(s):  
Zhibin Guo ◽  
Ruijie Xiu ◽  
Shanfu Lu ◽  
Xin Xu ◽  
Shichun Yang ◽  
...  

A novel submicro-pore containing proton exchange membrane is designed and fabricated for application in high-temperature fuel cells.


Energies ◽  
2020 ◽  
Vol 13 (6) ◽  
pp. 1383 ◽  
Author(s):  
Liping Fan ◽  
Junyi Shi ◽  
Tian Gao

Proton exchange membrane is an important factor affecting the power generation capacity and water purification effect of microbial fuel cells. The performance of microbial fuel cells can be improved by modifying the proton exchange membrane by some suitable method. Microbial fuel cells with membranes modified by SiO2/PVDF (polyvinylidene difluoride), sulfonated PVDF and polymerized MMA (methyl methacrylate) electrolyte were tested and their power generation capacity and water purification effect were compared. The experimental results show that the three membrane modification methods can improve the power generation capacity and water purification effect of microbial fuel cells to some extent. Among them, the microbial fuel cell with the polymerized MMA modified membrane showed the best performance, in which the output voltage was 39.52 mV, and the electricity production current density was 18.82 mA/m2, which was 2224% higher than that of microbial fuel cell with the conventional Nafion membrane; and the COD (chemical oxygen demand) removal rate was 54.8%, which was 72.9% higher than that of microbial fuel cell with the conventional Nafion membrane. Modifying the membrane with the polymerized MMA is a very effective way to improve the performance of microbial fuel cells.


Sign in / Sign up

Export Citation Format

Share Document